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Andrew J. Armstrong, MD, professor of medicine, associate professor in pharmacology and cancer biology, and professor in surgery at Duke University School of Medicine and a member of the Duke Cancer Institute, discusses the potential of AR-V7 as a predictive biomarker of response to taxane chemotherapy in metastatic castration-resistant prostate cancer (mCRPC).
Andrew J. Armstrong, MD, professor of medicine, associate professor in pharmacology and cancer biology, and professor in surgery at Duke University School of Medicine and a member of the Duke Cancer Institute, discusses the potential of AR-V7 as a predictive biomarker of response to taxane chemotherapy in metastatic castration-resistant prostate cancer (mCRPC).
Men with progressive mCRPC can receive either a second-generation androgen receptor (AR) inhibitor or taxane chemotherapy in the second-line setting. Many patients do not want to experience the adverse events associated with chemotherapy even though it may be more beneficial to them, says Armstrong. As such, having a biomarker that could predict for response to these treatments could help patients decide between the 2 approaches.
In the study, investigators evaluated AR-V7 as a predictive biomarker of response to taxane chemotherapy. Investigators concluded that AR-V7 is a negative biomarker of response to abiraterone and enzalutamide. Additionally, patients, irrespective of AR-V7 status, benefitted from docetaxel or cabazitaxel in the second- or third-line setting, says Armstrong. Testing for AR-V7 in practice could help patients decide between these approaches; however, the absence of AR-V7 does not confer response to AR inhibitors, concludes Armstrong.